Evidence map›Paper›PMID 42063069›Full record

ArticleJournal of translational medicine2026

Mesenchymal Stem cell therapy with GHRH receptor analog resolves post-stroke vasogenic edema via modulating AQP4 and mitochondria-ER crosstalk.

Aishika Datta, Bijoyani Ghosh, Anita Kumari, Gautam Karmarkar, Ushmita Mukherjee, Akshada Dubey, Anirban Barik, Ankit Singh, Nikita Malik, Deepaneeta Sarmah and 5 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Aishika DattaDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Bijoyani GhoshDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Anita KumariDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Gautam KarmarkarDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Ushmita MukherjeeDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Akshada DubeyDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Anirban BarikDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Ankit SinghDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Nikita MalikDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Deepaneeta SarmahDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India.
Andrew V SchallyDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL, USA.
Medhi WangpaichitrDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL, USA.
Wei ShaDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL, USA.
Dileep R YavagalDepartment of Neurology and Neurosurgery, Miller School of Medicine, University of Miami, Miami, FL, USA.
Pallab BhattacharyaDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gandhinagar, Gujarat, 382355, India. pallab.bhu@gmail.com.ORCID 0000-0003-2867-1650

Funding

Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, India Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, IndiaGujarat State Biotechnology Mission (GSBTM) PID:202526_20Indian Council of Medical Research 45/13/2020-PHA/BMSIndian Council of Medical Research IIRP-2023-3905/F1
6 · The paper itself

Abstract

backgroundPost-stroke edema is one of the fatal consequences of ischemic stroke where increased intracranial pressure can exacerbate neurological dysfunction leading to mortality. To date, conventional post-stroke therapy has failed to manage cerebral edema and render neuroprotection. Earlier, our lab reported the benefits of intra-arterially administered mesenchymal stem cells (IA MSCs) in alleviating post-stroke vasogenic edema. Recently, post-stroke neuroendocrine regulation involving growth hormone releasing hormone receptor (GHRH-R) analog is gaining attention as one of the potential targets for stroke intervention, adjunctive to the existing conventional therapies. Therefore, the current study aims to explore the combined therapeutic potential of IA MSCs and GHRH-R analogs in resolution of cerebral vasogenic edema following ischemic stroke.

methodsMiddle cerebral artery occlusion (MCAo) method was used to induce focal ischemic stroke in male Sprague Dawley rats. Further rats were treated with 1 × 10

resultsPost-stroke administration of IA MSCs and MR-409 combination reduced mitochondria-endoplasmic reticulum (ER) distance, modulated AQP4 expression, leading to reduction in blood-brain-barrier (BBB) disruption in the short term along with resolving vasogenic edema in the long term.

conclusionThe study provides indirect preliminary evidence of combined administration of IA MSCs with sustained release GHRH-R agonist towards increasing the mitochondria-endoplasmic reticulum association, altering the expression of AQP4, maintaining BBB integrity and alleviating post-stroke vasogenic edema.

Indexed as

Aquaporin 4Brain EdemaEndoplasmic ReticulumMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMitochondriaReceptors, NeuropeptideReceptors, Pituitary Hormone-Regulating HormoneStrokeAnimalsInfarction, Middle Cerebral ArteryMaleRats, Sprague-DawleyAquaporin 4Receptors, NeuropeptideReceptors, Pituitary Hormone-Regulating Hormonesomatotropin releasing hormone receptorAquaporinsGrowth-hormone releasing hormone receptor analogsIschemic strokeMesenchymal stem cellsMitochondria-endoplasmic reticulum crosstalkVasogenic edema

Identifiers

PMID42063069
PMCPMC13154448

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.